10/28/2018
A Contract Research Organisation (CRO), established by ACDIMA to provide principally bioequivalence testing services to the pharmaceutical industry Founded in 2000 and headquartered in Amman-Jordan, the heart of Middle East Located in a nicely placed area within the west region of the capital Amman accessible to all visitors. Provides a tailor-made service to support your challenging regulatory needs with cost-effective prices and in a very short time. Gained an excellent reputation since its foundation with its multinational presentation. Considered the largest CRO in the MENA region. Aligning study timelines to meet your deadlines with a very short project cycle time: IMP importation & Custom clearance: 1-7 days IRB review /approval: 1 week Regulatory approval: 1-4 weeks Screening: 1-3 days Study conduct: 1-4 weeks Bioanalysis: 2-3 weeks Preliminary results: 1 week Final report: 1 week
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